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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

CLOFARABINE for Bone marrow conditioning regimen: Side Effects & Safety Data

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There are 160 adverse event reports in the FDA FAERS database where CLOFARABINE was used for Bone marrow conditioning regimen.

Most Reported Side Effects for CLOFARABINE

Side Effect Reports % Deaths Hosp.
Febrile neutropenia 201 14.2% 57 85
Off label use 158 11.1% 78 39
Drug ineffective 139 9.8% 43 33
Pyrexia 139 9.8% 25 50
Mucosal inflammation 89 6.3% 13 5
Sepsis 85 6.0% 46 24
Alanine aminotransferase increased 82 5.8% 14 18
Acute kidney injury 80 5.6% 54 20
Multiple organ dysfunction syndrome 77 5.4% 72 25
Aspartate aminotransferase increased 76 5.4% 13 15
Neutropenia 76 5.4% 24 19
Pancytopenia 69 4.9% 27 23
Haematotoxicity 67 4.7% 10 1
Product use in unapproved indication 66 4.7% 23 16
Bone marrow failure 63 4.4% 37 13

Other Indications for CLOFARABINE

Acute myeloid leukaemia (357) Acute lymphocytic leukaemia (323) Acute lymphocytic leukaemia recurrent (71) Chemotherapy (48) Product used for unknown indication (43) Langerhans' cell histiocytosis (37) B precursor type acute leukaemia (35) Allogenic stem cell transplantation (31) Stem cell transplant (26) Acute lymphocytic leukaemia refractory (25)

Other Drugs Used for Bone marrow conditioning regimen

FLUDARABINE (6,080) BUSULFAN (4,669) CYCLOPHOSPHAMIDE (4,485) MELPHALAN (2,368) LAPINE T-LYMPHOCYTE IMMUNE GLOBULIN (1,884) THIOTEPA (1,551) ALEMTUZUMAB (1,122) ETOPOSIDE (936) CYTARABINE (833) THYMOCYTE IMMUNE GLOBULIN NOS (742)

Related Pages

CLOFARABINE Full Profile All Bone marrow conditioning regimen Drugs CLOFARABINE Demographics CLOFARABINE Timeline